HBG2

hemoglobin subunit gamma 2
OMIM: 142250, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Red HBG2 in Cytopenias and congenital anaemias

Level 3: Anaemias and red cell disorders
Level 2: Haematological disorders
Version 1.118

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • BRIDGE consortium (NIHRBR-RD)
Phenotypes
  • Fetal hemoglobin quantitative trait locus 1, OMIM:141749
  • Cyanosis, transient neonatal, OMIM:613977
  • Globin Disorder
Green HBG2 in Rare anaemia


Version 3.8
Latest signed off version: v3.0 (22 Mar 2023)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • North West GLH
  • Yorkshire and North East GLH
  • London South GLH
  • NHS GMS
  • Expert Review Green
  • Wessex and West Midlands GLH
Phenotypes
  • Fetal hemoglobin quantitative trait locus 1, OMIM:141749
  • Cyanosis, transient neonatal, OMIM:613977
  • Globin Disorder
Amber HBG2 in Haemoglobinopathy trait or carrier testing


Version 1.7
Latest signed off version: v1.0 (14 Sep 2023)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • NHS GMS
Tags
  • Q4_23_promote_green
Amber HBG2 in Thalassaemia and other haemoglobinopathies


Version 1.7
Latest signed off version: v1.0 (14 Sep 2023)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • NHS GMS
Tags
  • Q4_23_promote_green